Automated production of [<sup>68</sup>Ga]Ga-DOTA-exendin-4 via fractionated radionuclide generator elution on a cassette based synthesis module.
Nucl Med Biol · 2023
Last updated 2026-05-28Researchers developed an automated system to produce a radioactive imaging drug called [Ga]Ga-DOTA-exendin-4, which helps detect insulinomas using PET/CT scans. The process used a commercial generator and a synthesis module, achieving over 93% purity in batches and maintaining stability for at least 2 hours after production. The final product contained less than 1 milligram per milliliter of polysorbate 80, a common additive. The method was tested successfully in 5 master batches, confirming its reliability for routine clinical use.
AI summary of the abstract below.
| Journal | Nucl Med Biol, 2023 |
|---|---|
| Citations | 1 |
| Relative citation ratio | 0.13 |
| NIH percentile | 9 |
| Molecules | — |
Abstract
BACKGROUND: PET/CT imaging of glucagon-like peptide receptor 1 has recently filled a gap in reliably diagnosing insulinoma through non-invasive means. Ga-labelled derivatives of exendin-4 show high sensitivity as well as sufficient serum stability to enable routine clinical application. Here, we provide data for automated production of [Ga][Nle,Lys(Ahx-DOTA-Ga)NH]exendin-4 ([Ga]Ga-DOTA-exendin-4) on a cassette based synthesis module (Modular-Lab PharmTracer, Eckert & Ziegler) using commercially available cassettes in combination with an approved Ge/Ga generator (GalliaPharm, Eckert & Ziegler). This setup ensured high reproducibility as well as low radiation burden for the production team. Quality control including determination of radiochemical purity was performed by RP-HPLC using a water/0.1 % TFA/acetonitrile gradient on a C18 column. A modified TLC system with ammonium acetate & methanol as mobile phase and a novel limit test for determination of polysorbate 80 content in the final formulation are also described in this study.
MAIN FINDINGS: Reliable yields as well as high molar activity for patient use were only achieved using a fractionated elution approach. Batch data showed radiochemical purity of >93 % as determined by RP-HPLC and TLC as well as good stability over 2 h post production. Testing for polysorbate 80 confirmed a concentration <1 mg/mL in the final product solution. Specifications for routine production were established based on existing Pharmacopeia monographs for other radiopharmaceuticals and were validated with 5 master batches.
CONCLUSION: The described synthesis method enables reproducible, automated in-house production of [Ga]Ga-DOTA-exendin-4 for routine clinical application.
Verbatim abstract via PubMed 37634398 ↗